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Nature Communications|October 11, 2018
A missense variant in SLC39A8 is associated with severe idiopathic scoliosisGabe Haller, Kevin McCall, Supak Jenkitkasemwong, et al.American Journal of Human Genetics|December 22, 2020
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.Pageof 2